Canonical Allele Identifier: CA341808238

Gene: VTCN1

Linked Data

• MyVariant Identifiers: chr1:g.117690345C>G (hg19) ; chr1:g.117147723C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.117147723C>G , CM000663.2:g.117147723C>G	GRCh38
NC_000001.10:g.117690345C>G , CM000663.1:g.117690345C>G	GRCh37
NC_000001.9:g.117491868C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369458.8:c.784G>C MANE Select	ENSP00000358470.3:p.Val262Leu
ENST00000328189.7:c.436G>C	ENSP00000328168.3:p.Val146Leu
ENST00000359008.8:c.793G>C	ENSP00000351899.4:p.Val265Leu
ENST00000369458.7:c.784G>C	ENSP00000358470.3:p.Val262Leu
ENST00000539893.5:c.499G>C	ENSP00000444724.1:p.Val167Leu
NM_001253849.1:c.499G>C	NP_001240778.1:p.Val167Leu
NM_001253850.1:c.436G>C	NP_001240779.1:p.Val146Leu
NM_024626.3:c.784G>C	NP_078902.2:p.Val262Leu
NR_045603.1:n.979G>C
NR_045604.1:n.683G>C
XM_011542143.1:c.835G>C	XP_011540445.1:p.Val279Leu
XM_011542144.1:c.838G>C	XP_011540446.1:p.Val280Leu
XM_011542145.1:c.799G>C	XP_011540447.1:p.Val267Leu
XM_011542143.2:c.934G>C	XP_011540445.2:p.Val312Leu
XM_017002335.2:c.799G>C	XP_016857824.1:p.Val267Leu
NM_024626.4:c.784G>C MANE Select	NP_078902.2:p.Val262Leu
NR_045603.2:n.946G>C
NR_045604.2:n.650G>C
NM_001253849.2:c.499G>C	NP_001240778.1:p.Val167Leu
NM_001253850.2:c.436G>C	NP_001240779.1:p.Val146Leu